Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06804785

Hybrid Intelligence for Trustable Diagnosis and Patient Management of Prostate Cancer (HIT-PIRADS)

The purpose of this study is to develop a new way to diagnose prostate cancer through the use of artificial intelligence. The goal is for this new method to reduce delays in diagnoses and to avoid invasive procedures such as biopsies.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–89 year

Sex eligibility

Male

Study type

Observational

Primary location

National Institutes of Health

Bethesda, Maryland, 20892, United States

Location status: Recruiting

Location contact

Ismail Turkbey

CONTACT

mailto:[email protected]

240-760-6112

About this study

The overall goal of this project is to create a diagnosis and patient management strategy (called HIT-PIRADS) for prostate cancer (PCa) that will significantly increase positive predictive value (PPV) for clinically significant PCa detection while minimizing unnecessary prostate biopsies and related morbidities. Due to its interpretable nature and bias correction paradigm, the AI system will generate predictions that physicians can trust. One of the immediate outcomes of the system will be a reproducible risk scoring system that can be used in community hospitals and locales without MRI-subspeciality genitourinary trained radiologists to improve the accuracy of prostate imaging nationwide. In the long term, the investigators expect HIT-PIRADS to be widely adopted in clinics and trigger other treatment and prevention strategies to be developed based on HIT-PIRADS.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Elevated PSA (4.0-10.0 ng/ml) or abnormal digital rectal exam with PSA of 2.00-10.00 ng/ml as indicated in the patient's lab report.
  • Patients must be biopsy naïve, confirmed with patient or medical record.
  • Patients must be male, ≥18 and ≤ 89 years of age.
  • Patient must have a life expectancy ≥10 years, determined by PI.
  • Patients must exhibit an ECOG performance status of 0-2, as noted in their medical record.

Exclusion criteria

  • Patients who are on a 5-α-reductase inhibitor within 12 months of enrollment, as confirmed by medical record.
  • Patients who have had a prostate infection within 1 month of enrollment, as confirmed by medical record.
  • Patients who are receiving or who received prostate cancer treatment (e.g., androgen deprivation therapy, surgery, radiation therapy or adjuvant/neoadjuvant therapy with investigational drugs) per their medical record.
  • Patients who've had an invasive urological procedure within 1 month of enrollment, as confirmed by their medical record and patient reporting.
  • Patients with no access to the rectum for a transrectal ultrasound, as determined by the Urologist.
  • Patients with a contraindication to magnetic resonance imaging (MRI).
  • Vulnerable populations: Prisoners or adult men >89 years old.

Treatment and study plan

Primary outcomes

  1. Number of Participants with detection of clinically significant prostate cancer (csPCa)

    Time frame: 01/01/2016-12/31/2026

    csPCa is defined as PCa with a Gleason Grade Group of 2 through 5 found on prostate biopsy. Detection of csPCa will be compared for HITPIRADS vs. PIRADS v2.1 with a focus on suspicious lesions.

Study contacts

Contact information is provided by the study sponsor or research team.

Ismail Turkbey

CONTACT

[email protected]

240.760.6112

Sponsors and collaborators

Lead sponsor

Northwestern University

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Acronym: HIT-PIRADS

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
Feb 3, 2025
Registry last updated
May 31, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.